Canonical Allele Identifier: CA1465794638
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670475C= , CM000666.2:g.68670475C= GRCh38
NC_000004.11:g.69536193C= , CM000666.1:g.69536193C= GRCh37
NC_000004.10:g.69218788C= NCBI36
NG_052676.1:g.5302G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.144G= MANE Select ENSP00000341045.5:p.Gln48=
ENST00000338206.5:c.144G= ENSP00000341045.5:p.Gln48=
ENST00000616841.4:c.144G= ENSP00000482004.1:p.Gln48=
NM_001076.3:c.144G= NP_001067.2:p.Gln48=
NM_001076.4:c.144G= MANE Select NP_001067.2:p.Gln48=